相关参考文献
注意:仅列出部分参考文献,下载原文获取全部文献信息。Fusion production of solid dispersions containing a heat-sensitive active ingredient by hot melt extrusion and Kinetisol® dispersing
James C. DiNunzio et al.
EUROPEAN JOURNAL OF PHARMACEUTICS AND BIOPHARMACEUTICS (2010)
Fusion Processing of Itraconazole Solid Dispersions by KinetiSol® Dispersing: A Comparative Study to Hot Melt Extrusion
James C. DiNunzio et al.
JOURNAL OF PHARMACEUTICAL SCIENCES (2010)
Molecular Aspects of Mucoadhesive Carrier Development for Drug Delivery and Improved Absorption
Nicholas A. Peppas et al.
JOURNAL OF BIOMATERIALS SCIENCE-POLYMER EDITION (2009)
Towards quantitative prediction of oral drug absorption
Jennifer B. Dressman et al.
CLINICAL PHARMACOKINETICS (2008)
Enhanced in vivo absorption of itraconazole via stabilization of supersaturation following acidic-to-neutral pH transition
Dave A. Miller et al.
DRUG DEVELOPMENT AND INDUSTRIAL PHARMACY (2008)
Hydroxyitraconazole, formed during intestinal first-pass metabolism of itraconazole, controls the time course of hepatic CYP3A inhibition and the Bioavailability of itraconazole in rats
Sara K. Quinney et al.
DRUG METABOLISM AND DISPOSITION (2008)
Ordered mesoporous silica induces pH-independent supersaturation of the basic low solubility compound itraconazole resulting in enhanced transepithelial transport
Randy Mellaerts et al.
INTERNATIONAL JOURNAL OF PHARMACEUTICS (2008)
Gut instincts: Explorations in intestinal physiology and drug delivery
Emma L. McConnell et al.
INTERNATIONAL JOURNAL OF PHARMACEUTICS (2008)
Measurements of rat and mouse gastrointestinal pH fluid and lymphoid tissue, and implications for in-vivo experiments
Emma L. McConnell et al.
JOURNAL OF PHARMACY AND PHARMACOLOGY (2008)
Amorphous Compositions Using Concentration Enhancing Polymers for Improved Bioavailability of Itraconazole
James C. DiNunzio et al.
MOLECULAR PHARMACEUTICS (2008)
Bioavailability and Bioequivalence: Focus on physiological factors and variability
Vangelis Karalis et al.
PHARMACEUTICAL RESEARCH (2008)
Targeted intestinal delivery of supersaturated itraconazole for improved oral absorption
Dave A. Miller et al.
PHARMACEUTICAL RESEARCH (2008)
Effect of stabilizer on the maximum degree and extent of supersaturation and oral absorption of tacrolimus made by ultra-rapid freezing
Kirk A. Overhoff et al.
PHARMACEUTICAL RESEARCH (2008)
Pharmacokinetics of itraconazole after intravenous and oral dosing of itraconazole-cyclodextrin formulations
Charles M. Buchanan et al.
JOURNAL OF PHARMACEUTICAL SCIENCES (2007)
Combined use of crystalline salt forms and precipitation inhibitors to improve oral absorption of celecoxib from solid oral formulations
Hector R. Guzman et al.
JOURNAL OF PHARMACEUTICAL SCIENCES (2007)
Use of a screening method to determine excipients which optimize the extent and stability of supersaturated drug solutions and application of this system to solid formulation design
Roger Vandecruys et al.
INTERNATIONAL JOURNAL OF PHARMACEUTICS (2007)
Estimating drug solubility in the gastrointestinal tract
J. B. Dressman et al.
ADVANCED DRUG DELIVERY REVIEWS (2007)
Part II: Bioavailability in beagle dogs of nimodipine solid dispersions prepared by hot-melt extrusion
Xin Zheng et al.
DRUG DEVELOPMENT AND INDUSTRIAL PHARMACY (2007)
Supersaturation produces high bioavailability of amorphous danazol particles formed by evaporative precipitation into aqueous solution and spray freezing into liquid technologies
JM Vaughn et al.
DRUG DEVELOPMENT AND INDUSTRIAL PHARMACY (2006)
Carbopol-mediated paracellular transport enhancement in Calu-3 cell layers
LL Li et al.
JOURNAL OF PHARMACEUTICAL SCIENCES (2006)
Nanoparticle formulation increases oral bioavailability of poorly soluble drugs: Approaches, experimental evidences and theory
L Jia
CURRENT NANOSCIENCE (2005)
Physicochemical characterization and mechanisms of release of theophylline from melt-extruded dosage forms based on a methacrylic acid copolymer
CR Young et al.
INTERNATIONAL JOURNAL OF PHARMACEUTICS (2005)
Bioavailability enhancement of a COX-2 inhibitor, BMS-347070,, from a nanocrystalline dispersion prepared by spray-drying
SX Yin et al.
JOURNAL OF PHARMACEUTICAL SCIENCES (2005)
Clinical study of solid dispersions of itraconazole prepared by hot-stage extrusion
K Six et al.
EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES (2005)
Pharmaceutical Aspects of Polymeric Nanoparticles for Oral Drug Delivery
V. Bhardwaj et al.
JOURNAL OF BIOMEDICAL NANOTECHNOLOGY (2005)
Molecular weight determination of hypromellose acetate succinate (HPMCAS) using size exclusion chromatography with a multi-angle laser light scattering detector
M Fukasawa et al.
CHEMICAL & PHARMACEUTICAL BULLETIN (2004)
Enhanced oral bioavailability of a poorly water soluble drug PNU-91325 by supersaturatable formulations
P Gao et al.
DRUG DEVELOPMENT AND INDUSTRIAL PHARMACY (2004)
Development of a supersaturable SEDDS (S-SEDDS) formulation of paclitaxel with improved oral bioavailability
P Gao et al.
JOURNAL OF PHARMACEUTICAL SCIENCES (2003)
Establishment of new preparation method for solid dispersion formulation of tacrolimus
K Yamashita et al.
INTERNATIONAL JOURNAL OF PHARMACEUTICS (2003)
Formulation of amphotericin B as nanosuspension for oral administration
O Kayser et al.
INTERNATIONAL JOURNAL OF PHARMACEUTICS (2003)
Characterization of the Interaction of 2-hydroxypropyl-β-cyclodextrin with itraconazole at pH 2, 4, and 7
J Peeters et al.
JOURNAL OF PHARMACEUTICAL SCIENCES (2002)
Intestinal drug efflux: formulation and food effects
D Wagner et al.
ADVANCED DRUG DELIVERY REVIEWS (2001)
Itraconazole oral solution and intravenous formulations: a review of pharmacokinetics and pharmacodynamics
L Willems et al.
JOURNAL OF CLINICAL PHARMACY AND THERAPEUTICS (2001)
Characterization of glassy itraconazole:: a comparative study of its molecular mobility below Tg with that of structural analogues using MTDSC
K Six et al.
INTERNATIONAL JOURNAL OF PHARMACEUTICS (2001)